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PROPHYFLEX 2, MODEL 2012

Page Type
Cleared 510(K)
510(k) Number
K973876
510(k) Type
Traditional
Applicant
KAVO AMERICA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/1997
Days to Decision
70 days
Submission Type
Statement

PROPHYFLEX 2, MODEL 2012

Page Type
Cleared 510(K)
510(k) Number
K973876
510(k) Type
Traditional
Applicant
KAVO AMERICA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/1997
Days to Decision
70 days
Submission Type
Statement